首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Estimation of rotavirus immunoglobulin G antibodies in human serum samples by enzyme-linked immunosorbent assay: expression of results as units derived from a standard curve.
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Estimation of rotavirus immunoglobulin G antibodies in human serum samples by enzyme-linked immunosorbent assay: expression of results as units derived from a standard curve.

机译:通过酶联免疫吸附测定法估算人血清中的轮状病毒免疫球蛋白G抗体:以标准曲线为单位表示结果。

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摘要

A method for estimating rotavirus immunoglobulin G (IgG) antibodies by assay of human serum samples at a single serum dilution was studied. Antibody was measured by enzyme-linked immunosorbent assay (ELISA). The optical density of the reaction with a 1:100 dilution of each serum was expressed as ELISA units of antirotavirus IgG by reference to a standard curve. This standard curve was obtained by incorporation in each assay of five dilutions of a serum containing an arbitrary number of units of antirotavirus IgG. Test serum samples found to contain high amounts of antirotavirus IgG were reassayed at a 1:1,000 dilution. There was good correlation between antirotavirus IgG ELISA units in 45 serum samples and endpoint titers of the same samples (Spearman rank correlation coefficient rs, 0.95). Seroconversion during rotavirus infection was defined as an increase in antirotavirus IgG ELISA units per milliliter of greater than 28% (2 X intra-run coefficient of variation of the assay) in consecutive serum samples from the same child. Paired serum samples from nine children with diarrhea not due to rotavirus infection showed no seroconversions. Paired samples from eight children with rotavirus infection showed seroconversions. Estimation of antirotavirus IgG ELISA units in serum is simple, rapid, reproducible, and economical of serum samples. Standardization of results could be achieved by worldwide distribution of a standard serum. Its use would facilitate epidemiological surveys to evaluate potential rotavirus vaccines.
机译:研究了一种通过在单一血清稀释液中检测人血清样品来估计轮状病毒免疫球蛋白G(IgG)抗体的方法。通过酶联免疫吸附测定(ELISA)测量抗体。参照标准曲线,将各血清以1:100稀释的反应的光密度表示为抗轮状病毒IgG的ELISA单位。通过在每种测定法中加入五种稀释液(包含任意数量的抗轮状病毒IgG)来获得该标准曲线。发现含有大量抗轮状病毒IgG的测试血清样品以1:1,000的稀释度重新测定。 45个血清样品中的抗轮状病毒IgG ELISA单位与相同样品的终点滴度之间具有良好的相关性(Spearman等级相关系数rs,0.95)。轮状病毒感染期间的血清转化被定义为来自同一儿童的连续血清样本中每毫升每毫升抗轮状病毒IgG ELISA单位的增加大于28%(分析的运行内变异系数的2 X)。来自非轮状病毒感染的9例腹泻儿童的配对血清样本未显示血清转化。来自八名轮状病毒感染儿童的配对样本显示出血清转化。血清中抗轮状病毒IgG ELISA单位的估算简单,快速,可重现,并且经济高效。结果的标准化可以通过在全球范围内分发标准血清来实现。它的使用将有助于流行病学调查,以评估潜在的轮状病毒疫苗。

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